Identity
- Trade Name
- EXEL SRGCL BLADE,S-S, SIZE:11 EUDAMEDFDA UDIEXEL Surgical Blade, Stainless Steel Size 11 EUDAMED
- Generic Name
- Manual scalpel blade, single-use FDA UDI
- Device Name
- EXEL SURGICAL BLADE EUDAMEDEXEL SRGCL BLADE,S-S, SIZE:11; 100/BX, 1000/CS, 10CS/CRTN FDA UDI
- Model / Reference
- 29502 EUDAMEDFDA UDI
- Description
- EXEL SRGCL BLADE,S-S, SIZE:11; 100/BX, 1000/CS, 10CS/CRTN FDA UDI
Identifiers
- Catalog Number
- 29502 FDA UDI
- Primary DI / UDI-DI
- 00020221295023 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00020221295023 EUDAMED20221SURGBL295J4 EUDAMED
- FDA Product Code
- GES FDA UDI
- EMDN Code
- V010302 BLADES WITHOUT SAFETY SYSTEMS, SINGLE-USE - NOT INCLUDED IN OTHER CLASSES EUDAMEDV010102 SCALPELS WITHOUT SAFETY SYSTEMS, SINGLE-USE EUDAMED
- GMDN Term
- Manual scalpel blade, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Market of Registration
- Netherlands EUDAMEDAustria EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Exel Srgcl Blade, S-S, Size:11 by Exelint International, Co. — Class IIa — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | B-00020221295023 | Class IIa | Active |
| EUDAMED | European Union | CE/MDD | B-00020221295023 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Exelint International, Co.
- EUDAMED SRN
- US-MF-000037396
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (3)
- EUDAMED a1f7b6b7-6319-49bb-8a0a-9f6235488b4d 61 fields · synced Jul 15, 2026
- FDA UDI cd6c34a4-e185-4d33-bd2c-c3e9a8cf5b69 35 fields · synced May 29, 2026
- EUDAMED 010da7d5-3519-4571-bb9e-bc920392636d 61 fields · synced Jul 15, 2026